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Author Details
Full Name
Yijun Huang
Affiliation
University of Wisconsin, Wisconsin EyeKor Inc.
ORCID
Career Start Year
1997
Papers
16
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32679202
Quantification of Geographic Atrophy Using Spectral Domain OCT in Age-Related Macular Degeneration.
Ophthalmol Retina
2021
27128499
Variability in Spectral-Domain Optical Coherence Tomography over 4 Weeks by Age.
Ophthalmic Epidemiol
2016
25556116
The epidemiology of vitreoretinal interface abnormalities as detected by spectral-domain optical coherence tomography: the beaver dam eye study.
Ophthalmology
2015
25461295
Retinal thickness measured by spectral-domain optical coherence tomography in eyes without retinal abnormalities: the Beaver Dam Eye Study.
Am J Ophthalmol
2015
23761091
Effect of optical coherence tomography scan decentration on macular center subfield thickness measurements.
Invest Ophthalmol Vis Sci
2013
24386127
Development of a semi-automatic segmentation method for retinal OCT images tested in patients with diabetic macular edema.
PLoS One
2013
22427567
Signal quality assessment of retinal optical coherence tomography images.
Invest Ophthalmol Vis Sci
2012
10634630
Psychophysical evidence for rod vulnerability in age-related macular degeneration.
Invest Ophthalmol Vis Sci
2000
10655151
Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degeneration.
Exp Eye Res
2000
10440267
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.
Invest Ophthalmol Vis Sci
1999
10449795
Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina.
Proc Natl Acad Sci U S A
1999
9804149
Relation of optical coherence tomography to microanatomy in normal and rd chickens.
Invest Ophthalmol Vis Sci
1998
9804150
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.
Invest Ophthalmol Vis Sci
1998
9618546
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.
Proc Natl Acad Sci U S A
1998
9331262
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
Invest Ophthalmol Vis Sci
1997
9286267
Rod plateaux during dark adaptation in Sorsby's fundus dystrophy and vitamin A deficiency.
Invest Ophthalmol Vis Sci
1997
1 - 16 of 16
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Cynthia A Toth
Duke University School of Medicine
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Casey Eye Institute, Oregon Health & Science University
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Dirk-Uwe Bartsch
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row(s) 1 - 30 of 30
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Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
Co-authored papers
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Ronald P Danis
University of Wisconsin, Wisconsin EyeKor Inc.
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7
Ronald Klein
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5
Amitha Domalpally
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Co-authored papers
2
Edwin M Stone
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2
James A Knowles
Co-authored papers
1
Virginia R Lolley
Heersink School of Medicine, University of Alabama at Birmingham
Co-authored papers
1
Maureen G Maguire
Perelman School of Medicine, University of Pennsylvania
Co-authored papers
1
Allen C Ho
Wills Eye Hospital/Mid Atlantic Retina
Co-authored papers
1
Cynthia Owsley
University of Alabama at Birmingham
Co-authored papers
1
Anand Swaroop
National Eye Institute, National Institutes of Health
Co-authored papers
1
Stuart L Fine
Kaiser Permanente San Francisco Medical Center
Co-authored papers
1
Carol L Freund
the Center for Genetics and Health Policy, Vanderbilt University Medical School
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1
Guangping Gao
Co-authored papers
1
Gregory R Jackson
b MacuLogix Inc.
Co-authored papers
1
Donald J Zack
Johns Hopkins University School of Medicine
Co-authored papers
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1 - 17